Evidence map›Paper›PMID 39285465›Full record

ArticleNeuropsychopharmacology reports2024

Clozapine treatment of a Japanese patient during pregnancy: Effect on fetal heart rate.

Shunya Aoki, Katsutoshi Takada, Tatsuru Sugama, Mitsugi Kimiwada, Tatsuya Hoshino, Takaoki Kaneko, Shintaro Obata, Yasuhiro Ota, Satoshi Toishi, Kaori Koike and 3 more

Abstract readCase Reports
In one paragraph

Article in Neuropsychopharmacology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Shunya AokiPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.ORCID 0009-0005-6539-1932
Katsutoshi TakadaPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Tatsuru SugamaPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Mitsugi KimiwadaPharmaceutical Department, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Tatsuya HoshinoNursing Department, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Takaoki KanekoDepartment of Obstetrics and Gynecology, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Shintaro ObataDepartment of Obstetrics and Gynecology, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Yasuhiro OtaDepartment of Neonatology, Japanese Red Cross Narita Hospital, Chiba, Japan.
Satoshi ToishiDepartment of Neonatology, Japanese Red Cross Narita Hospital, Chiba, Japan.
Kaori KoikeDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Hirokazu AkadaDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Takahisa SaigaDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Shigeki SatoDepartment of Psychiatry, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current literature on the effects of clozapine on pregnancy is limited, and no cases of pregnant Japanese women have been reported. Decreased variability in the fetal heart rate due to clozapine exposure has been reported in countries other than Japan, but its association with serum concentrations of clozapine has not been documented. In this case, a 29-year-old Japanese primipara with treatment-resistant schizophrenia taking clozapine 250 mg/day experienced pregnancy. The pregnancy progressed without complications. At 40 weeks and 2 days of gestation, the patient developed premature rupture of membranes, and decreased variability in the fetal heart rate and variable deceleration were observed, leading to an emergency cesarean section. The neonate had no congenital malformations, metabolic disorders, seizures, floppy infant syndrome, leukopenia, or neutropenia. Serum concentrations of clozapine and norclozapine (N-desmethylclozapine), measured in the mother and in the neonate immediately after birth, suggested that clozapine and norclozapine were transported to the fetus during pregnancy. Based on these observations, the present case suggests that high fetal serum concentrations of clozapine and norclozapine may affect fetal heart rate. This case report concludes that, with careful monitoring, Japanese women taking clozapine can deliver successfully and emphasizes the importance of monitoring serum clozapine concentrations and fetal cardiac function throughout pregnancy, with particular attention to the later stages.

Indexed as

Antipsychotic AgentsClozapineHeart Rate, FetalPregnancy ComplicationsAdultEast Asian PeopleFemaleHumansInfant, NewbornJapanPregnancySchizophrenia, Treatment-ResistantAntipsychotic AgentsClozapineclozapinedrug monitoringJapanese peoplematernal‐fetal exchangepregnancy

Identifiers

PMID39285465
PMCPMC11609758

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.